Canonical Allele Identifier: CA688734074

Gene: LRRK2

Linked Data

• dbSNP Id: rs1555196691
• MyVariant Identifiers: chr12:g.40757114_40757115insGCAT (hg19) ; chr12:g.40363312_40363313insGCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363312_40363313insGCAT , CM000674.2:g.40363312_40363313insGCAT	GRCh38
NC_000012.11:g.40757114_40757115insGCAT , CM000674.1:g.40757114_40757115insGCAT	GRCh37
NC_000012.10:g.39043381_39043382insGCAT	NCBI36
NG_011709.1:g.143302_143303insGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-90_7029-89insGCAT MANE Select	ENSP00000298910.7:n.7029-90_7029-89insGCAT
ENST00000636518.1:c.826-90_826-89insGCAT
ENST00000679360.1:c.*5938-90_*5938-89insGCAT	ENSP00000505368.1:n.*5938-90_*5938-89insGCAT
ENST00000679532.1:c.2803-90_2803-89insGCAT
ENST00000679683.1:c.819-90_819-89insGCAT
ENST00000680018.1:c.2474-90_2474-89insGCAT	ENSP00000505347.1:n.2474-90_2474-89insGCAT
ENST00000680422.1:c.4116-90_4116-89insGCAT
ENST00000680425.1:c.2196-90_2196-89insGCAT	ENSP00000506459.1:n.2196-90_2196-89insGCAT
ENST00000680453.1:c.2486-90_2486-89insGCAT
ENST00000680790.1:c.6774-90_6774-89insGCAT	ENSP00000505335.1:n.6774-90_6774-89insGCAT
ENST00000681136.1:n.3013-90_3013-89insGCAT
ENST00000681696.1:c.2712-90_2712-89insGCAT	ENSP00000505871.1:n.2712-90_2712-89insGCAT
ENST00000681773.1:n.236-90_236-89insGCAT
ENST00000298910.11:c.7029-90_7029-89insGCAT	ENSP00000298910.7:n.7029-90_7029-89insGCAT
ENST00000430804.5:c.4325-90_4325-89insGCAT
ENST00000479187.5:n.3710-90_3710-89insGCAT
NM_198578.3:c.7029-90_7029-89insGCAT	NP_940980.3:n.7029-90_7029-89insGCAT
XM_005268629.2:c.7029-90_7029-89insGCAT	XP_005268686.1:n.7029-90_7029-89insGCAT
XM_011537877.1:c.7029-90_7029-89insGCAT	XP_011536179.1:n.7029-90_7029-89insGCAT
XM_011537878.1:c.*787_*788insGCAT	XP_011536180.1:n.*787_*788insGCAT
XM_011537879.1:c.5826-90_5826-89insGCAT	XP_011536181.1:n.5826-90_5826-89insGCAT
XR_944868.1:n.485-8486_485-8485insATGC
XM_005268629.4:c.7029-90_7029-89insGCAT	XP_005268686.1:n.7029-90_7029-89insGCAT
XM_011537877.3:c.7029-90_7029-89insGCAT	XP_011536179.1:n.7029-90_7029-89insGCAT
XM_017018787.1:c.3945-90_3945-89insGCAT	XP_016874276.1:n.3945-90_3945-89insGCAT
XM_017018788.2:c.3291-90_3291-89insGCAT	XP_016874277.1:n.3291-90_3291-89insGCAT
XM_024448833.1:c.5826-90_5826-89insGCAT	XP_024304601.1:n.5826-90_5826-89insGCAT
XR_944868.2:n.485-8486_485-8485insATGC
NM_198578.4:c.7029-90_7029-89insGCAT MANE Select	NP_940980.4:n.7029-90_7029-89insGCAT